FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP

K Number: K020170 · Decision Feb 11, 2002
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
85
Review Days
25

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Basic Information

Device Name
KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
K Number
K020170
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Orthopedics, Inc.
Date Received
January 17, 2002
Decision Date
February 11, 2002
Product Code
LPH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LPH), ordered by most recent decision date.

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Other Clearances by Encore Orthopedics, Inc.

K Number Device Name
K032905 3DKNEE POROUS COATED FEMORAL COMPONENT
K020114 3D KNEE
K020741 UNICONDYLAR KNEE
K020236 MODIFICATION TO PASS SPINAL SYSTEM
K013490 CEMENTED CALCAR HIP SYSTEM
K013442 PASS SPINAL SYSTEM
K003324 PLASMA SPRAYED SHOULDER
K013431 PASS SPINAL SYSTEM
K013191 PASS SPINAL SYSTEM
K011856 RADIOGRAPHIC MARKERS
Search all 85 clearances from Encore Orthopedics, Inc. →